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FDA 510(k)

DECHERNEY HYSTEROSCOPY PUMP SYSTEM

K-Number: K873527 · 1988-02-26

ApplicantCabot Medical Corp.
Decision Date1988-02-26
Product CodeHIG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DECHERNEY HYSTEROSCOPY PUMP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cabot Medical Corp.. It received FDA 510(k) clearance on 1988-02-26 under 510(k) number K873527. The device is classified under product code HIG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DECHERNEY HYSTEROSCOPY PUMP SYSTEM?

DECHERNEY HYSTEROSCOPY PUMP SYSTEM is a medical device that received FDA 510(k) clearance on 1988-02-26. The listed applicant is Cabot Medical Corp.. The 510(k) number is K873527.

When did DECHERNEY HYSTEROSCOPY PUMP SYSTEM receive FDA 510(k) clearance?

DECHERNEY HYSTEROSCOPY PUMP SYSTEM received FDA 510(k) clearance on 1988-02-26, under 510(k) number K873527.

Who is the listed applicant for DECHERNEY HYSTEROSCOPY PUMP SYSTEM?

The FDA 510(k) record lists Cabot Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DECHERNEY HYSTEROSCOPY PUMP SYSTEM?

The FDA product code for DECHERNEY HYSTEROSCOPY PUMP SYSTEM is HIG.

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Other records listing Cabot Medical Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K960148CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENTK946109CABOT MEDICAL REUSABLE BIPOLAR CUTTING FORCEPSK951972CABOT MEDICAL ULTRA FLOW CYSTOURETHROSCOPE SYSTEM WITH OPERATING & DIAGNOSTIC SHEATHSK951714CABOT MEDICAL-SURGITEK ULTRAGOLD PLUS SIDE-FIRING UROLOGIC LASER FIBERK941743CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMPK9341153000 ELECTRONIC INSUFFLATOR MODIFICATION

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Related Devices (Code: HIG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261706Endomat Select (UP220)KARL STORZ SE & CO. KGK251273Asurys Fluid Management SystemBoston Scientific CorporationK240886Fluent Pro Fluid Management System (FLT-200); Fluent Pro Fluid Management System Disposable Procedure Kit (6-pack) (FLT-212); Fluent Pro Fluid Management System Disposable Procedure Kit (1-pack) (FLT-212S); Fluent Pro Fluid Management System Tissue Trap Multipack (10-pack) (FLT-210); Fluent Pro Fluid Management System Waste Bag Multipack (5-pack) (FLT-205)Hologic, Inc.K210628X-FLO Fluid Management SystemThermedx, LLCK201355Endomat Select, IBS Shaver Software, LicenseKarl Storz SE & CO. KGK180735Endomat SelectKarl Storz SE & CO. KG

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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